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3 associated genes
4 signs/symptoms
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Narcolepsy without cataplexy
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

HCRT HNRNPA1
HLA-DQB1 HNRNPA2B1
HLA-DRB1 VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HLA-DRB1
(0.63)
VCP



Citations in the biomedical literature:


Narcolepsy without cataplexy
HCRT HLA-DQB1 HLA-DRB1
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
HNRNPA1 HNRNPA2B1 VCP



Narcolepsy without cataplexy
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Synonym(s):
(no synonyms)

Synonym(s):
- IBMPFD
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid amyotrophic lateral sclerosis
- Pagetoid neuroskeletal syndrome

Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references

Narcolepsy without cataplexy

Very frequent
- Delirium / hallucination
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia

Occasional
- Psychic / behavioural troubles


Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

(no data available)